-
Je něco špatně v tomto záznamu ?
Impact of three-month morphine withdrawal on rat brain cortex, hippocampus, striatum and cerebellum: proteomic and phosphoproteomic studies
H. Ujcikova, L. Hejnova, A. Eckhardt, L. Roubalova, J. Novotny, P. Svoboda
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- abstinenční syndrom genetika metabolismus MeSH
- časové faktory MeSH
- corpus striatum účinky léků metabolismus MeSH
- fosforylace fyziologie MeSH
- hipokampus účinky léků metabolismus MeSH
- krysa rodu rattus MeSH
- morfin škodlivé účinky MeSH
- mozeček účinky léků metabolismus MeSH
- mozková kůra účinky léků metabolismus MeSH
- poruchy spojené s užíváním opiátů genetika metabolismus MeSH
- potkani Wistar MeSH
- proteomika metody MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Opioid addiction is characterized by compulsive drug seeking and taking behavior, which is thought to result from persistent neuroadaptations. However, there is a lack of information about the changes at both the cellular and molecular levels occurring after cessation of drug administration. The aim of our study was to determine alterations of both phosphoproteome and proteome in selected brain regions of the rats (brain cortex, hippocampus, striatum, and cerebellum) 3 months after cessation of 10-day morphine treatment. Phosphoproteome profiling was performed by Pro-Q® Diamond staining. The gel-based proteomic approach accompanied by label-free quantification (MaxLFQ) was used for characterization of proteome changes. The phosphoproteomic analysis revealed the largest change in the hippocampus (14); only few altered proteins were detected in the forebrain cortex (5), striatum (4), and cerebellum (3). The change of total protein composition, determined by 2D electrophoresis followed by LFQ analysis, identified 22 proteins with significantly altered expression levels in the forebrain cortex, 19 proteins in the hippocampus, 12 in the striatum and 10 in the cerebellum. The majority of altered proteins were functionally related to energy metabolism and cytoskeleton reorganization. As the most important change we regard down-regulation of 14-3-3 proteins in rat cortex and hippocampus. Our findings indicate that i) different parts of the brain respond in a distinct manner to the protracted morphine withdrawal, ii) characterize changes of protein composition in these brain parts, and iii) enlarge the scope of evidence for adaptability and distinct neuroplasticity proceeding in the brain of drug-addicted organism.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc22004591
- 003
- CZ-PrNML
- 005
- 20220127145133.0
- 007
- ta
- 008
- 220113s2021 xxk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.neuint.2021.104975 $2 doi
- 035 __
- $a (PubMed)33508371
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxk
- 100 1_
- $a Ujcikova, Hana $u Laboratory of Membrane Receptors, Department of Biomathematics, Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 142 20, Prague 4, Czech Republic. Electronic address: Hana.Ujcikova@fgu.cas.cz
- 245 10
- $a Impact of three-month morphine withdrawal on rat brain cortex, hippocampus, striatum and cerebellum: proteomic and phosphoproteomic studies / $c H. Ujcikova, L. Hejnova, A. Eckhardt, L. Roubalova, J. Novotny, P. Svoboda
- 520 9_
- $a Opioid addiction is characterized by compulsive drug seeking and taking behavior, which is thought to result from persistent neuroadaptations. However, there is a lack of information about the changes at both the cellular and molecular levels occurring after cessation of drug administration. The aim of our study was to determine alterations of both phosphoproteome and proteome in selected brain regions of the rats (brain cortex, hippocampus, striatum, and cerebellum) 3 months after cessation of 10-day morphine treatment. Phosphoproteome profiling was performed by Pro-Q® Diamond staining. The gel-based proteomic approach accompanied by label-free quantification (MaxLFQ) was used for characterization of proteome changes. The phosphoproteomic analysis revealed the largest change in the hippocampus (14); only few altered proteins were detected in the forebrain cortex (5), striatum (4), and cerebellum (3). The change of total protein composition, determined by 2D electrophoresis followed by LFQ analysis, identified 22 proteins with significantly altered expression levels in the forebrain cortex, 19 proteins in the hippocampus, 12 in the striatum and 10 in the cerebellum. The majority of altered proteins were functionally related to energy metabolism and cytoskeleton reorganization. As the most important change we regard down-regulation of 14-3-3 proteins in rat cortex and hippocampus. Our findings indicate that i) different parts of the brain respond in a distinct manner to the protracted morphine withdrawal, ii) characterize changes of protein composition in these brain parts, and iii) enlarge the scope of evidence for adaptability and distinct neuroplasticity proceeding in the brain of drug-addicted organism.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a mozeček $x účinky léků $x metabolismus $7 D002531
- 650 _2
- $a mozková kůra $x účinky léků $x metabolismus $7 D002540
- 650 _2
- $a corpus striatum $x účinky léků $x metabolismus $7 D003342
- 650 _2
- $a hipokampus $x účinky léků $x metabolismus $7 D006624
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a morfin $x škodlivé účinky $7 D009020
- 650 _2
- $a poruchy spojené s užíváním opiátů $x genetika $x metabolismus $7 D009293
- 650 _2
- $a fosforylace $x fyziologie $7 D010766
- 650 _2
- $a proteomika $x metody $7 D040901
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a potkani Wistar $7 D017208
- 650 _2
- $a abstinenční syndrom $x genetika $x metabolismus $7 D013375
- 650 _2
- $a časové faktory $7 D013997
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Hejnova, Lucie $u Department of Physiology, Faculty of Science, Charles University, Vinicna 7, 128 43, Prague 2, Czech Republic
- 700 1_
- $a Eckhardt, Adam $u Laboratory of Translational Metabolism, Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 142 20, Prague 4, Czech Republic
- 700 1_
- $a Roubalova, Lenka $u Laboratory of Membrane Receptors, Department of Biomathematics, Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 142 20, Prague 4, Czech Republic
- 700 1_
- $a Novotny, Jiri $u Department of Physiology, Faculty of Science, Charles University, Vinicna 7, 128 43, Prague 2, Czech Republic
- 700 1_
- $a Svoboda, Petr $u Laboratory of Membrane Receptors, Department of Biomathematics, Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 142 20, Prague 4, Czech Republic
- 773 0_
- $w MED00003485 $t Neurochemistry international $x 1872-9754 $g Roč. 144, č. - (2021), s. 104975
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/33508371 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20220113 $b ABA008
- 991 __
- $a 20220127145129 $b ABA008
- 999 __
- $a ok $b bmc $g 1751905 $s 1155740
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 144 $c - $d 104975 $e 20210127 $i 1872-9754 $m Neurochemistry international $n Neurochem Int $x MED00003485
- LZP __
- $a Pubmed-20220113